Drug products
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Thallous Chloride Tl 201
Active Ingredient CEFIXIME Proprietary Name SUPRAX Applicant LEDERLE Dosage Form;Route ORAL Strength 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or Application Type N Product Number 1 Approval Date 1989/04/28 RX/OTC/DISCN No Applicant Full Name DISCN
FDA's Approved Drug Products database
